(Q30655446)

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Toward high-throughput genotyping: dynamic and automatic software for manipulating large-scale genotype data using fluorescently labeled dinucleotide markers

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scholarly article

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Europe PubMed Central

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20 September 2017

Toward high-throughput genotyping: dynamic and automatic software for manipulating large-scale genotype data using fluorescently labeled dinucleotide markers (English)

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Europe PubMed Central

PMC publication ID

20 September 2017

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H Deng

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Robert R. Recker

7

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R R Recker

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J L Li

1

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Europe PubMed Central

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20 September 2017

D B Lai

3

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Europe PubMed Central

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20 September 2017

F Xu

4

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Europe PubMed Central

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20 September 2017

J Chen

5

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Europe PubMed Central

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20 September 2017

G Gao

6

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Europe PubMed Central

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20 September 2017

R R Recker

7

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Europe PubMed Central

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20 September 2017

H W Deng

8

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20 September 2017

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1 July 2001

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20 September 2017

Genome Research

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20 September 2017

11

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20 September 2017

7

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Europe PubMed Central

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20 September 2017

1304-1314

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Europe PubMed Central

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20 September 2017

Using quality measures to facilitate allele calling in high-throughput genotyping

1 reference

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New reference allelic ladders to improve allelic designation in a multiplex STR system.

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20 June 2018

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

1 reference

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20 June 2018

Integrating clinical and laboratory data in genetic studies of complex phenotypes: a network-based data management system

1 reference

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20 June 2018

Multipoint quantitative-trait linkage analysis in general pedigrees

1 reference

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20 June 2018

A simple method for automated allele binning in microsatellite markers

1 reference

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20 June 2018

An approach to high-throughput genotyping

1 reference

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20 June 2018

PhenoDB: an integrated client/server database for linkage and population genetics

1 reference

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20 June 2018

The geneticist's approach to complex disease

1 reference

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Parametric and nonparametric linkage analysis: a unified multipoint approach

1 reference

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20 June 2018

Identification of repeat sequence heterogeneity at the polymorphic short tandem repeat locus HUMTH01[AATG]n and reassignment of alleles in population analysis by using a locus-specific allelic ladder

1 reference

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20 June 2018

Genetic dissection of complex traits

1 reference

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20 June 2018

Toward fully automated genotyping: allele assignment, pedigree construction, phase determination, and recombination detection in Duchenne muscular dystrophy

1 reference

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20 June 2018

Toward fully automated genotyping: genotyping microsatellite markers by deconvolution.

1 reference

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20 June 2018

Is Population Bone Mineral Density Variation Linked to the Marker D11S987 On Chromosome 11q12–13?

1 reference

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25 November 2018

Genetic determination of Colles' fracture and differential bone mass in women with and without Colles' fracture

1 reference

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25 November 2018

Determination of bone mineral density of the hip and spine in human pedigrees by genetic and life-style factors

1 reference

https://pubmed.ncbi.nlm.nih.gov/11435414

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterogeneity of bone mineral density across skeletal sites and its clinical implications

1 reference

https://pubmed.ncbi.nlm.nih.gov/11435414

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers. FUSION (Finland-U.S. Investigation of NIDDM Genetics) Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/11435414

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations

1 reference

https://pubmed.ncbi.nlm.nih.gov/11435414

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1101/GR.159701

1 reference

Europe PubMed Central

PMC publication ID

20 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 September 2017

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